Teguh Citra Asmara

A fundamental understanding of the interplay between lattice structure, polarization and electrons is pivotal to the optical control of ferroelectrics. The interaction between light and matter enables the remote and wireless control of the ferroelectric polarization on the picosecond timescale, while inducing strain, i.e., lattice deformation. At equilibrium, the ferroelectric polarization is proportional to the strain, and is typically assumed to be so also out of equilibrium. Decoupling the polarization from the strain would remove the constraint of sample design and provide an effective knob to manipulate the polarization by light. Here, upon above-bandgap laser excitation of the prototypical ferroelectric BaTiO₃, we induce and measure an ultrafast decoupling between polarization and strain that begins within 350 fs, by softening Ti-O bonds via charge transfer, and lasts for several tens of picoseconds. We show that the ferroelectric polarization out of equilibrium is mainly determined by photoexcited electrons, instead of the strain.

Honeycomb and kagome lattices can host propagating excitations with non-trivial topology as defined by their evolution along closed paths in momentum space. Excitations on such lattices can also be momentum-independent, and the associated flat bands are of interest due to strong interactions between heavy quasiparticles. Here, we report the discovery — using circularly polarized X-rays for the unambiguous isolation of magnetic signals — of a nearly flat spin-wave band and large (compared to elemental iron) orbital moment in the metallic ferromagnet Fe₃Sn₂ with compact AB-stacked kagome bilayers. As a function of out-of-plane momentum, the nearly flat optical mode and the global rotation symmetry-restoring acoustic mode are out of phase, consistent with a bilayer exchange coupling that is larger than the already large in-plane couplings. The defining units of this topological metal are therefore triangular lattices of octahedral iron clusters rather than weakly coupled kagome planes. The spin waves are strongly damped when compared to elemental iron, opening the topic of topological boson–fermion interactions for deeper exploration within this material platform.

Strongly‐correlated transition‐metal oxides are widely known for their various exotic phenomena. This is exemplified by rare‐earth nickelates such as LaNiO₃, which possess intimate interconnections between their electronic, spin, and lattice degrees of freedom. Their properties can be further enhanced by pairing them in hybrid heterostructures, which can lead to hidden phases and emergent phenomena. An important example is the LaNiO₃/LaTiO₃ superlattice, where an interlayer electron transfer has been observed from LaTiO₃ into LaNiO₃ leading to a high‐spin state. However, macroscopic emergence of magnetic order associated with this high‐spin state has so far not been observed. Here, by using muon spin rotation, x‐ray absorption, and resonant inelastic x‐ray scattering, direct evidence of an emergent antiferromagnetic order with high magnon energy and exchange interactions at the LaNiO₃/LaTiO₃ interface is presented. As the magnetism is purely interfacial, a single LaNiO₃/LaTiO₃ interface can essentially behave as an atomically thin strongly‐correlated quasi‐2D antiferromagnet, potentially allowing its technological utilization in advanced spintronic devices. Furthermore, its strong quasi‐2D magnetic correlations, orbitally‐polarized planar ligand holes, and layered superlattice design make its electronic, magnetic, and lattice configurations resemble the precursor states of superconducting cuprates and nickelates, but with an S→1 spin state instead.

Vibrationally-resolved resonant inelastic X-ray scattering (VR-RIXS) at the O K-edge is emerging as a powerful tool for identifying embedded molecules in lithium-ion battery cathodes. Here, we investigate two known oxygen redox-active cathode materials: the commercial Li_xNi_0.90Co_0.05Al_0.05O₂ (NCA) used in electric vehicles and the high-capacity cathode material Li_1.2Ni_0.13Co_0.13Mn_0.54O₂ (LRNMC) for next-generation Li-ion batteries. We report the detection of a novel vibrational RIXS signature for Li-ion battery cathodes appearing in the O K pre-peak above 533 eV that we attribute to OH-groups. We discuss likely locations and pathways for OH-group formation and accumulation throughout the active cathode material. Initial-cycle behaviour for LRNMC shows that OH-signal strength correlates with the cathodes state of charge, though reversibility is incomplete. The OH-group RIXS signal strength in long-term cycled NCA is retained. Thus, VR-RIXS offers a path for gaining new insights to oxygen reactions in battery materials.

In high-temperature cuprate superconductors, stripe order refers broadly to a coupled spin and charge modulation with a commensuration of eight and four lattice units, respectively. How this stripe order evolves across optimal doping remains a controversial question. Here we present a systematic resonant inelastic x-ray scattering study of weak charge correlations in La_2−xSr_xCuO₄ and La_1.8−xEu_0.2Sr_xCuO₄. Ultra high energy resolution experiments demonstrate the importance of the separation of inelastic and elastic scattering processes. Long-range temperature-dependent stripe order is only found below optimal doping. At higher doping, short-range temperature-independent correlations are present up to the highest doping measured. This transformation is distinct from and preempts the pseudogap critical doping. We argue that the doping and temperature-independent short-range correlations originate from unresolved electron–phonon coupling that broadly peaks at the stripe ordering vector. In La_2−xSr_xCuO₄, long-range static stripe order vanishes around optimal doping and we discuss both quantum critical and crossover scenarios.

The nature of the spin excitations in superconducting cuprates is a key question toward a unified understanding of the cuprate physics from long-range antiferromagnetism to superconductivity. The intense spin excitations up to the over-doped regime revealed by resonant inelastic X-ray scattering bring new insights as well as questions like how to understand their persistence or their relation to the collective excitations in ordered magnets (magnons). Here, we study the evolution of the spin excitations upon hole-doping the superconducting cuprate Bi₂Sr₂CaCu₂O_8+δby disentangling the spin from the charge excitations in the experimental cross section. We compare our experimental results against density matrix renormalization group calculations for at-J-like model on a square lattice. Our results unambiguously confirm the persistence of the spin excitations, which are closely connected to the persistence of short-range magnetic correlations up to high doping. This suggests that the spin excitations in hole-doped cuprates are related to magnons—albeit short-ranged.

We studied the magnetic excitations in the quasi-one-dimensional (q-1D) ladder subsystem of Sr_14−xCa_xCu₂₄O₄₁ (SCCO) using Cu L₃-edge resonant inelastic X-ray scattering (RIXS). By comparing momentum-resolved RIXS spectra with high (x = 12.2) and without (x = 0) Ca content, we track the evolution of the magnetic excitations from collective two-triplon (2 T) excitations (x = 0) to weakly-dispersive gapped modes at an energy of 280 meV (x = 12.2). Density matrix renormalization group (DMRG) calculations of the RIXS response in the doped ladders suggest that the flat magnetic dispersion and damped excitation profile observed at x = 12.2 originates from enhanced hole localization. This interpretation is supported by polarization-dependent RIXS measurements, where we disentangle the spin-conserving ΔS = 0 scattering from the predominant ΔS = 1 spin-flip signal in the RIXS spectra. The results show that the low-energy weight in the ΔS = 0 channel is depleted when Sr is replaced by Ca, consistent with a reduced carrier mobility. Our results demonstrate that off-ladder impurities can affect both the low-energy magnetic excitations and superconducting correlations in the CuO₄ plaquettes. Finally, our study characterizes the magnetic and charge fluctuations in the phase from which superconductivity emerges in SCCO at elevated pressures.

The superconducting critical temperature T_c of intercalated iron-selenide superconductor (Li,Fe)OHFeSe (FeSe11111) can be increased to 42 from 8 K of bulk FeSe. It shows remarkably similar electronic properties as the high-T_c monolayer FeSe and provides a bulk counterpart to investigate the origin of enhanced superconductivity. Unraveling the nature of excitations is crucial for understanding the pairing mechanism in high-T_c iron selenides. Here we use resonant inelastic x-ray scattering (RIXS) to investigate the excitations in FeSe11111. Our high-quality data exhibit several Raman-like excitations, which are dispersionless and isotropic in momentum transfer in both superconducting 28 K and 42 K samples. Using atomic multiplet calculations, we assign the low-energy ~0.3 and 0.7 eV Raman peaks as local e_g − e_g and e_g − t_2g orbital excitations. The intensity of these two features decreases with increasing temperature, suggesting a dominating contribution of the orbital fluctuations. Our results highlight the importance of the orbital degree of freedom for high-T_c iron selenides.